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Detecting Adverse Events Following Acute Care Encounters among Veterans Prescribed Non-Steroidal Anti-Inflammatory
Amber J Hackstadt1,2, Amy M Perkins1,2, Jesse O Wrenn3,4,5
1Geriatric Research Education and Clinical Care Center (GRECC) & VETWISE-LHS COIN, Tennessee Valley Healthcare System VA, Nashville, Tennessee, USA.
Nonsteroidal anti-inflammatory drugs (NSAIDs) pose risks for adverse events (AEs) in Veterans. Advanced models identified gastroesophageal reflux disease and advanced chronic kidney disease as key risk factors for NSAID-related AEs.
Area of Science:
- Pharmacovigilance
- Health Informatics
- Clinical Epidemiology
Background:
- Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly prescribed but carry risks for adverse events (AEs), including gastrointestinal, renal, and cardiovascular complications.
- These risks are amplified in vulnerable populations such as older adults, patients with chronic kidney disease (CKD), and those on polypharmacy.
- Understanding AE occurrence within specific healthcare systems like the Veterans Health Administration (VHA) is crucial for targeted interventions.
Purpose of the Study:
- To develop and evaluate predictive models for adverse events (AEs) in Veterans prescribed nonsteroidal anti-inflammatory drugs (NSAIDs).
- To identify specific risk factors associated with NSAID-related AEs within the VHA.
- To assess the performance of machine learning models in predicting AEs in this population.
Main Methods:
- Utilized eXtreme Gradient Boosting (XGBoost), LASSO regression, and logistic regression to model AE occurrence.
- Defined AEs as a composite outcome including acute coronary syndrome, acute kidney injury, allergic reactions, gastrointestinal bleeding, or GERD within 2-30 days post-encounter.
- Evaluated model performance using Area Under the Receiver Operating Characteristic Curve (AUC) and calibration plots, calculating observed-to-expected (OE) ratios.
Main Results:
- Analyzed 1,112,819 encounters for 736,677 unique Veterans, identifying 50,278 (4.5%) AEs.
- XGBoost and LASSO models demonstrated strong performance with AUC values between 0.77 and 0.79.
- Gastroesophageal reflux disease (GERD) and advanced CKD (stage 4-5/dialysis) were significantly associated with increased AE risk; OE ratios varied by VHA site.
Conclusions:
- Risk adjustment models exhibited good discrimination and identified significant site-specific variations in NSAID-related AEs.
- These predictive models show potential utility for clinical decision support systems.
- The findings support the development of targeted population health interventions to mitigate NSAID-associated risks.
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